Ng Beverly Cheok Kuan, Lassere Marissa
Department of Rheumatology, St George Hospital, Australia; University of New South Wales, School of Public Health and Community Medicine, Australia.
Department of Rheumatology, St George Hospital, Australia; University of New South Wales, School of Public Health and Community Medicine, Australia.
Semin Arthritis Rheum. 2025 Feb;70:152574. doi: 10.1016/j.semarthrit.2024.152574. Epub 2024 Oct 31.
There is an increasing body of literature observing a state of dysbiosis in the gut microbiome in different autoimmune conditions including inflammatory arthritis. It is unknown whether the microbiome can be a biomarker for prognostication purposes or for stratification of treatment strategies. This review aims to evaluate the existing evidence on the association between the microbiome and inflammatory arthritis, including rheumatoid arthritis (RA), psoriatic arthritis (PsA) and ankylosing spondylitis (AS) and reactive arthritis (ReA) population groups.
This systematic review was performed based on methods from the Cochrane guidelines and reported based on PRISMA criteria. Studies exploring the microbiome of patients with RA, AS, PsA or ReA compared with controls via 16s rRNA or shotgun sequencing were evaluated. The outcomes of interest include alpha and beta diversity, abundance or depletion of organisms and functional analysis. Literature up to August 2024 was retrieved searching the databases PubMed, Medline, ScienceDirect, Scopus, Web of Science, Cochrane, EMBASE and CINAHL. All references were systematically evaluated by two reviewers. Quality of the studies were evaluated by the Newcastle-Ottawa Scale.
The review yielded 25,794 search results, of which 53 studies were included for the RA group, 34 studies for the AS group, 6 studies for the PsA group and 2 studies for the ReA group. Reduced diversity has been observed in disease groups and in patients with higher disease activity.
There are limited longitudinal studies on the role of the microbiome in inflammatory arthritis, in particular PsA. Existing cross-sectional studies suggest altered microbiome in disease states compared with controls. Further studies are required to understand the utility of the microbiome as a biomarker to better understand prognosis and tailor treatments.
越来越多的文献观察到,在包括炎性关节炎在内的不同自身免疫性疾病中,肠道微生物群存在失调状态。尚不清楚微生物群是否可作为预后或治疗策略分层的生物标志物。本综述旨在评估关于微生物群与炎性关节炎(包括类风湿性关节炎(RA)、银屑病关节炎(PsA)、强直性脊柱炎(AS)和反应性关节炎(ReA)人群组)之间关联的现有证据。
本系统综述基于Cochrane指南的方法进行,并根据PRISMA标准报告。评估了通过16s rRNA或鸟枪法测序将RA、AS、PsA或ReA患者的微生物群与对照组进行比较的研究。感兴趣的结果包括α和β多样性、生物体的丰度或减少以及功能分析。检索了截至2024年8月的文献,搜索了PubMed、Medline、ScienceDirect、Scopus、Web of Science、Cochrane、EMBASE和CINAHL数据库。所有参考文献均由两名审稿人进行系统评估。研究质量由纽卡斯尔-渥太华量表评估。
该综述产生了25,794条搜索结果,其中RA组纳入53项研究,AS组纳入34项研究,PsA组纳入6项研究,ReA组纳入2项研究。在疾病组和疾病活动度较高的患者中观察到多样性降低。
关于微生物群在炎性关节炎,特别是PsA中的作用的纵向研究有限。现有的横断面研究表明,与对照组相比,疾病状态下的微生物群发生了改变。需要进一步研究以了解微生物群作为生物标志物的效用,以便更好地理解预后并调整治疗方案。